Skip to content

Providing Evidence-Based Approaches for Caregiver Stress Study

Providing Evidence-Based Approaches for Caregiver Stress (PEACE) Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06451250
Acronym
PEACE
Enrollment
42
Registered
2024-06-11
Start date
2024-02-02
Completion date
2025-12-19
Last updated
2025-12-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caregiving Stress, Dementia

Brief summary

The purpose of this preliminary study is to examine the effects of adult day service use on subjective and physiological measures of stress in 50 Black informal caregivers for individuals with dementia (IWD). The PI of the proposed study has substantial training in primary data collection and complex-survey secondary data analysis, she also has the fundamental knowledge to investigate how sociocultural and behavioral factors can influence psychosocial stress. The proposed study will enroll participants from adult day service (ADS) nationally, to examine the effects of adult day service use on subjective and physiological measures of stress in 50 Black informal caregivers. The proposed study extends the current science on the use of ADS on subjective and physiological stress by 1) examining differential impacts of ADS specifically on subjective measures of stress for Black caregivers, 2) evaluating the impact of ADS use on physiological measures of stress among Black caregivers; and 3) examining the relationship between subjective indicators and physiological processes for Black caregivers.

Interventions

OTHERAdult Day Service use for family member with dementia

Self-collection of salivary biomarkers 4 times daily for 5 days, two of those days the family member with dementia has to use adult day services

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
Johns Hopkins Bloomberg School of Public Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years or older (male or female) * Self-identify as Black and/or African American, * Lives with a family member with a physician diagnosis of Alzheimer's disease or related dementia * Primary responsibility for care of the family member who has been diagnosed with Alzheimer's disease or related dementia * Utilize Adult Day Services at least two times a week for family member with Alzheimer's disease or related dementia

Exclusion criteria

* Either caregiver of client is in active treatment for a terminal illness or are in hospice.

Design outcomes

Primary

MeasureTime frameDescription
Caregiver stress as assessed by the Perceived Stress ScaleBaselinePerceived Stress Scale scores range from 0 to 40 with higher scores indicating higher perceived stress

Secondary

MeasureTime frameDescription
Salivary cortisol levelsOver a five day periodSaliva will be collected into sterile collection tubes and stored in participants' freezers until sampling. the test volume will be 25 µL with a sensitivity range of 0.007-3.0 µL/dl.
Salivary alpha-amylaseOver a five day periodSaliva will be collected into sterile collection tubes and stored in participants' freezers until sampling. the test volume will be 10 µL with a sensitivity range of 0.4-400 U/mL.
Salivary Telomere lengthOver a five day periodSaliva will be collected into sterile collection tubes and stored in participants' freezers until sampling. the test volume will be 2ml

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026